CARNOY'S SOLUTION
K-Number: K842737 · 1984-09-07
Advertisement
Device Summary
Frequently Asked Questions
What is the CARNOY'S SOLUTION?
CARNOY'S SOLUTION is a medical device that received FDA 510(k) clearance on 1984-09-07. The listed applicant is E K Ind., Inc.. The 510(k) number is K842737.
When did CARNOY'S SOLUTION receive FDA 510(k) clearance?
CARNOY'S SOLUTION received FDA 510(k) clearance on 1984-09-07, under 510(k) number K842737.
Who is the listed applicant for CARNOY'S SOLUTION?
The FDA 510(k) record lists E K Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARNOY'S SOLUTION?
The FDA product code for CARNOY'S SOLUTION is IGM.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing E K Ind., Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IGM)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement